Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
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Supporting evidence
ID History
- Gene history

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Gene: NMD3 ENSPTRG00000015586

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Description

NMD3 ribosome export adaptor [Source:VGNC Symbol;Acc:VGNC:2448]

Location

Chromosome 3: 164,839,383-164,887,944 forward strand.

Pan_tro_3.0:CM000317.3

About this gene

This gene has 3 transcripts (splice variants) and 210 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000107869.1	NMD3-201	1767	529aa	ENSPTRP00000079947.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3SSN9	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical,
ENSPTRT00000029067.4	NMD3-202	3363	503aa	ENSPTRP00000026821.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2QNN7	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT2,
ENSPTRT00000086716.1	NMD3-203	1542	505aa	ENSPTRP00000085223.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3T8L8	APPRIS P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as the principal variant. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P5,

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Summary

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